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Business · 03/11/1999Updated: 10/17/2026 · 1 min read

FDA Denies QED, Inc. Petition to Reclassify Fiber Optic Light Sources

Summary

The FDA has rejected QED, Inc.'s request to reclassify fiber optic light sources used with endoscopes from Class II to Class I, citing a lack of new evidence to support the claim that general controls would ensure device safety and effectiveness.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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